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nsv6471319

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 181 SVs from 37 studies. See in: genome view    
    Submitted genomic89,496,401-89,533,900Question Mark
    Overlapping variant regions from other studies: 181 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):89,890,178-89,927,677Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6471319Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1289,496,40189,533,900
    nsv6471319RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1289,890,17889,927,677

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18193868duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18193868Submitted genomicNC_000012.12:g.894
    96401_89533900dup
    GRCh38 (hg38)NC_000012.12Chr1289,496,40189,533,900
    nssv18193868RemappedPerfectNC_000012.11:g.898
    90178_89927677dup
    GRCh37.p13First PassNC_000012.11Chr1289,890,17889,927,677

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18193868<0.0013439250
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